Canonical Allele Identifier: CA7203933

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.58271868A>T , CM000676.2:g.58271868A>T GRCh38
NC_000014.8:g.58738586A>T , CM000676.1:g.58738586A>T GRCh37
NC_000014.7:g.57808339A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000216455.9:c.741A>T (PSMA3) MANE Select ENSP00000216455.4:p.Glu247Asp
ENST00000216455.8:c.741A>T (PSMA3) ENSP00000216455.4:p.Glu247Asp
ENST00000412908.6:c.720A>T (PSMA3) ENSP00000390491.2:p.Glu240Asp
ENST00000553677.1:c.225A>T (PSMA3) ENSP00000450573.1:p.Glu75Asp
ENST00000554218.1:n.258+19767T>A (ARMH4)
ENST00000557290.1:n.594A>T (PSMA3)
ENST00000557508.5:c.516A>T (PSMA3) ENSP00000452056.1:p.Glu172Asp
NM_002788.3:c.741A>T (PSMA3) NP_002779.1:p.Glu247Asp
NM_152132.2:c.720A>T (PSMA3) NP_687033.1:p.Glu240Asp
NR_029434.1:n.454+2111T>A (PSMA3-AS1)
NR_029435.1:n.413+2111T>A (PSMA3-AS1)
NR_038123.1:n.774A>T (PSMA3)
NM_002788.4:c.741A>T (PSMA3) MANE Select NP_002779.1:p.Glu247Asp
NM_152132.3:c.720A>T (PSMA3) NP_687033.1:p.Glu240Asp
NR_038123.2:n.736A>T (PSMA3)